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Medline is recalling 11 groups of surgical convenience kits. The kits contain a component that the manufacturer recalled because it may be contaminated. No injuries have been reported, and the kits were distributed in 18 states.

Moderate·FDA·Sep 2, 202611 products

Some ConMed Linvatec GENESYS CrossFT Suture Anchors (REF# CFBC-5502B, Lot 1513167) may contain an incorrect patient implant card. This card is used to identify and track the device after implantation, so an incorrect card could lead to confusion about which device was used.

Moderate·FDA·Sep 2, 2026·ConMed

Fresenius Medical Care has identified a problem with certain 2008T BlueStar hemodialysis machines that can cause flow, water supply, or temperature alarms to malfunction. These alarms are important safety features that alert clinical staff to problems during treatment. About 1,140 affected machines have been identified by serial number.

Moderate·FDA·Sep 2, 2026

Henry Schein is recalling two dental restorative products, Structur 2 SC Temporary Resin Cartridge Refill and Grandio Universal Nano-Hybrid Restorative Material Capsules, with 974 units affected. Specific lots were distributed in the U.S. and Barbados with incorrect packaging and Instructions for Use from the FDA-cleared device.

Moderate·FDA·Sep 2, 2026·Henry Schein2 products

Fixing screws on the ceiling movement gear of the suspended arm in Canon Medical Alphenix interventional X-ray systems may become loose over time. This could potentially cause the arm to shift during use. Ten systems are affected across eight U.S. states.

Moderate·FDA·Sep 2, 2026

Midmark is recalling two digital electrocardiogram (ECG) products, including the IQecg Digital ECG and the Digital ECG HD+12 and HD+15, because a communication anomaly may cause incorrect heart waveforms and an inaccurate beats-per-minute reading. The recall covers software versions of the IQecg Plugin starting with v10 and before v10.1.0.18. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Midmark2 products

AVID Medical is recalling seven Halyard medical kit products because the labeling does not disclose that the StatLock component contains natural rubber latex. The kits were distributed nationwide, including in Mississippi and Texas. No injuries have been reported.

Moderate·FDA·Sep 2, 20267 products

Merge Healthcare's PACS and OrthoPACS medical imaging workstations contain a software issue that may cause measurements to be displayed inaccurately. Version 9.5 is affected. The issue was identified in 20 units distributed across California, Florida, Kentucky, Nebraska, and Washington.

Moderate·FDA·Sep 2, 2026·Merge Healthcare

American Contract Systems is recalling 4 convenience kit models that contain Medline Red Rubber Intermittent Catheters. Medline found that representative samples did not meet applicable performance specifications. The kits were distributed in Iowa and Ohio, and no injuries have been reported.

Moderate·FDA·Sep 2, 20264 products

Medline Industries distributed 45 tracheostomy tube kits (SKU DYKM2330) with incorrect component labeling. The discrepancy between the kit label and its contents could lead to confusion during use. No injuries have been reported.

Moderate·FDA·Sep 2, 2026

Hollister has identified a manufacturing defect in select lots of Onli Hydrophilic Urethral Intermittent Catheters that may cause a protrusion on the catheter tip. This defect could lead to genitourinary trauma or bleeding during use.

Moderate·FDA·Sep 2, 2026·Hollister

Medline is recalling specific lots of its medical convenience kits that contain Pilling Wecksorb Neurosponges and Neurosponge Strips. The neurosponges may have endotoxin levels above specification. The recall covers four product groups, about 6,950 kits in total, distributed in several US states. No injuries have been reported.

Moderate·FDA·Sep 2, 20264 products

Philips Incisive CT scanners running software versions V4.5 or V5.0 may fail to start a clinical scan during Bolus Tracking imaging procedures. This could delay or prevent necessary diagnostic scans from being acquired.

Moderate·FDA·Sep 2, 2026

Africando Foods LLC's Alfredo Hot Sauce is missing wheat and soybean oil from its ingredient label. Wheat is present as a sub-ingredient in the chicken bouillon, and soybean oil was used but not listed. The affected product was distributed to wholesale and retail locations in Iowa, Kentucky, and Illinois.

Moderate·FDA·Sep 2, 2026

Horizon Organic 1% chocolate milk in 8 oz cartons (sold in 12-count and 18-count multipacks) may be spoiled. The affected products have best-by dates between January 28 and February 3, 2027, and were distributed across the United States.

Moderate·FDA·Sep 2, 2026·Horizon Organic

Upstate Niagara Cooperative's Mehadrin Chocolate Leben 6 oz cups may not have been properly pasteurized, which could allow harmful bacteria to survive. The affected product was distributed in New Jersey and has a use-by date of 10/14/26.

Moderate·FDA·Sep 2, 2026·Mehadrin

Byron White Formulas is recalling three herbal supplements sold as A-L Complex, A-P, and A-FNG, all in 1.0 fl. oz. (30 mL) bottles. The English labels do not list walnuts, which are in the product, so people with a walnut allergy may not know it is there. No injuries have been reported.

Moderate·FDA·Sep 2, 20263 products

Lidl is recalling two Eridanous Greek Style shortbread cookie products, 330 g each, because some packages have labels only in foreign languages. The cookies contain wheat, soy, milk, eggs and coconut, which are not listed in English on the label. The products were shipped to stores in DC, DE, GA, MD, NJ, NY, NC, PA, SC and VA.

Moderate·FDA·Sep 2, 20262 products

Marketside Tomato Bisque Soup Kit tested positive for Listeria monocytogenes, a bacteria that can cause serious illness. The affected product is a 14 oz ready-to-heat soup kit with UPC 1 94346474004 and a Best By date of 8/22/2026.

Moderate·FDA·Sep 2, 2026

Outshine Fruit Bar Watermelon 6-count packages (UPC 041548413624) may contain glass pieces. The affected products were distributed across 33 U.S. states and territories. The recall includes specific batch codes with best-before dates ranging from June 30, 2027 to July 31, 2027.

Moderate·FDA·Sep 2, 2026·Outshine6 products

Hikma Pharmaceuticals is recalling specific lots of Ramipril Capsules 10 mg because testing found higher-than-allowed levels of dicyclohexylurea, a process impurity. The affected lots are AC5470A and AC5470B, both expiring July 2027. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Hikma Pharmaceuticals

Apotex Corp. is recalling one lot of Paxil CR (paroxetine) 37.5mg extended-release tablets because the medication failed to meet dissolution specifications during 24-month stability testing. This means the tablets may not release the drug into the body as intended. The affected lot (TY9494, expiration 05/31/2027) was distributed nationwide.

Moderate·FDA·Sep 2, 2026

Mallinckrodt has recalled specific lots of Acthar Gel (repository corticotropin injection) due to the presence of glass and stopper pieces in the vials. This contamination could pose a risk if the affected medication is used. The recall affects 12,367 vials with lot numbers 1564-107 and 1564-107H, both expiring January 31, 2027.

Moderate·FDA·Sep 2, 2026·Mallinckrodt

FDA inspection found that Zicam Cold Remedy Medicated Nasal Swabs failed microbiological testing, meaning they may contain harmful microbes. The affected products were manufactured under conditions that did not meet federal safety standards. Specific lot numbers with expiration dates through August 2028 are involved.

Moderate·FDA·Sep 2, 2026·Arm & Hammer

Lupin Pharmaceuticals is recalling specific lots of Clobetasol Propionate Cream USP 0.05% because the active ingredient is not uniformly distributed throughout the product. This means some parts of the cream may contain too much or too little medication, which could affect how well it works.

Moderate·FDA·Sep 2, 2026

Accord Healthcare is recalling specific lots of levothyroxine sodium tablets (25 mcg) because they contain less active ingredient than labeled. Patients taking these tablets may not receive the full dose needed to manage their thyroid condition. The affected lots were distributed nationwide.

Moderate·FDA·Sep 2, 2026·Accord Healthcare12 products

Certain 2024–2026 Toyota Tacoma Hybrid, Tundra, RAV4 Hybrid, 4Runner, and 4Runner i-Force Max Hybrid models have an inaccurate load carrying capacity label. This incorrect weight information could lead owners to overload the vehicle, increasing crash risk.

Moderate·NHTSA·Sep 2, 2026

Certain 2027 Peterbilt 548 trucks have front brake valves and hoses that may be the wrong size. This can delay how quickly the rear brakes and trailer connection respond when the driver applies the brakes, increasing crash risk.

Moderate·NHTSA·Sep 1, 2026

Certain 2024 and 2025 Forest River transit buses have wheelchair lifts equipped with electrical contactors that may fail. If a contactor fails, the lift controls cannot stop the lift while it is moving with a passenger on board, increasing injury risk.

Moderate·NHTSA·Sep 1, 2026·Forest River Bus, LLC

Light Boy America is recalling certain 2020 and 2023 GBX12SK light towers because the trailer frame can bend at the tow bar, causing the light tower to detach while being towed. A detached light tower can become a hazard to other vehicles on the road.

Moderate·NHTSA·Sep 1, 2026·Light Boy America,Inc